FDA PMA
FDA Class 3
Approved
🇺🇸 United States
System, Laser, Transmyocardial Revascularization
PMA: P970029
·
Supplement: S025
·
Decision Jan 28, 2014
Classifications
1
FEI Numbers
2
Registration Numbers
2
Basic Information
- Device Name
- System, Laser, Transmyocardial Revascularization
- Trade Name
- PEARL 8.0 HANDPIECE
- PMA Number
- P970029
- Supplement Number
- S025
- Device Class
- FDA Class 3
- Product Code
- MNO
- Generic Name
- SYSTEM, LASER, TRANSMYOCARDIAL REVASCULARIZATION
- Medical Specialty
- Unknown
- Advisory Committee
- Cardiovascular
- Decision
- Approved
- Decision Code
- APPR
- Decision Date
- January 28, 2014
- Date Received
- November 26, 2013
- Supplement Type
- Normal 180 Day Track No User Fee
- Supplement Reason
- Postapproval Study Protocol - OSB
- Expedited Review
- N
Advisory Committee Statement
APPROVAL OF THE POST-APPROVAL STUDY PROTOCOL.
Classifications
This FDA Pre-Market Approval entry is associated with 1 FDA classification via its product code.
| Product Code | Device Name | Device Class | Medical Specialty |
|---|---|---|---|
| MNO | System, Laser, Transmyocardial Revascularization | FDA class 3 | Unknown |